HIV-1 protease inhibitors having gem-di-fluoro bicyclic P2-ligands
Various embodiments of the present invention relate to, among other things, compounds and methods of using those compounds to treat an HIV infection. The compounds of the various embodiments of the present invention provide, among other things, therapeutic agents having enhanced penetration capability across the blood-brain barrier, such that they can enter the CNS to treat an HIV-1 infection in the CNS.
1. A compound of the formula
or a pharmaceutically acceptable salt thereof, wherein
n is 1;
R 1 is phenyl which is unsubstituted or which bears a fluoro, hydroxymethyl, methoxy or
2-(morpholin-4-yl)ethoxy substituent at the 3- or 4-position, or is 3,5-difluorophenyl;
R 2 is 2-propyl or 2-fluoro-2-propyl; and
—X—R 3 is selected from the group consisting of —SO 2 —R 3 , —C(O)—N(R)—R 3 , —NH—SO 2 —R 3 , and
—NH—C(O)—OR 3 ;
in which R is selected from the group consisting of (1-6C)alkyl, aryl, heteroaryl, aryl(1-6C)alkyl or heteroaryl(1-6C)alkyl, each of which is optionally substituted; and
R 3 is selected from the group consisting of (1-6C)alkyl, aryl, heteroaryl, aryl(1-6C)alkyl or heteroaryl(1-6C)alkyl, each of which is optionally substituted.
2. The compound of claim 1 wherein —X—R 3 is —SO 2 —R 3 .
3. The compound of claim 1 , wherein R 3 is selected from the group consisting of 4-aminophenyl, 4-methoxyphenyl, 4-hydroxymethylphenyl, 3-fluoro-4-methoxyphenyl, 4-amino-3-fluorophenyl, 3,4-methylenedioxyphenyl, benzoxazole-6-yl bearing a methyl, methylsulfonyl, dimethylamino or —NH—R 4 group at the 2-position; benzothiazole-6-yl bearing a methyl, methylsulfonyl, dimethylamino or —NH—R 4 group at the 2-position; and
benzimidazole-5-yl bearing a methyl or —NH—R 4 group at the 2-position; and
R 4 is selected from the group consisting of methyl, prop-2-yl, cyclopropyl, isobutyl, tert-butyl, cyclobutyl, cyclopentyl, cyclohexyl, piperidin-4-yl, 1-methylpiperidin-4-yl, 1-(prop-2-yl) piperidin-4-yl and 1-cyclopentylpiperidin-4-yl.
4. The compound of claim 3 , wherein R 3 is selected from the group consisting of 4-aminophenyl, 4-methoxyphenyl, and 3-fluoro-4-methoxyphenyl.
5. The compound of claim 3 , wherein R 3 is 2-(prop-2-ylamino)benzoxazole-6-yl.
6. The compound of claim 3 , wherein R 3 is benzothiazole-6-yl bearing a methylsulfonyl, dimethylamino, 2-(prop-2-yl-amino)-, cyclopropylamino, isobutylamino, tert-butylamino, cyclohexylamino, piperidin-4-ylamino, or 1-cyclopentylpiperidin-4-ylamino group at the 2-position.
7. The compound of claim 1 , wherein R 2 is 2-propyl.
8. The compound of claim 1 , wherein R 1 is phenyl, 3-methoxyphenyl or 4-methoxyphenyl.
9. The compound of claim 8 wherein R 1 is phenyl.
10. The compound of claim 1 , wherein R is hydrogen or methyl.
11. The compound of claim 1 , wherein R 1 is phenyl, 3-methoxyphenyl or 4-methoxyphenyl; R 2 is 2-propyl or 2-fluoro-2-propyl; —X—R 3 is —SO 2 —R 3 ; and R 3 is selected from the group consisting of 4-aminophenyl, 4-methoxyphenyl, 3-fluoro-4-methoxyphenyl; 2-(prop-2-ylamino)benzoxazole-6-yl; and benzothiazole-6-yl bearing a methylsulfonyl, dimethylamino, 2-(prop-2-yl-amino)-, cyclopropylamino, isobutylamino, tert-butylamino, cyclohexylamino, piperidin-4-ylamino, or 1-cyclopentylpiperidin-4-ylamino group at the 2-position.
12. The compound of claim 1 selected from the group consisting of:
13. The compound of claim 1 selected from the group consisting of:
14. A pharmaceutical composition comprising one or more compounds of claim 1 and one or more carriers, diluents, or excipients, or a combination thereof.
15. A method for treating a patient in need of relief from an HIV infection, the method comprising the step of administering to a patient in need of relief from the HIV infection a therapeutically effective amount of one or more compounds of claim 1 .